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Can Difficult-to-Reuse Syringes Reduce the Spread of HIV Among Injection Drug Users? -Caulkins, Kaplan, Lurie, O’Connor & Ahn. Presented by: Arifa Sultana Zoila Guerra Vikram Sriram. Outline. Introduction Models Model I - One type of syringe Model II - Multiple type of syringe
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Can Difficult-to-Reuse Syringes Reduce the Spread of HIV Among Injection Drug Users?-Caulkins, Kaplan, Lurie, O’Connor & Ahn Presented by: Arifa Sultana Zoila Guerra Vikram Sriram
Outline • Introduction • Models • Model I - One type of syringe • Model II - Multiple type of syringe • Future work
Introduction • Principal cause of HIV • Prevention/controlling methods • Using syringes that is impossible to reuse. (may not be feasible) • Distributing Difficult-to-reuse (DTR) syringes
Design approaches for DTR • Syringes containing hydrophilic gel • Plungers disabled when reload • Needles disabled after the first use • Valves that prevent second loading
Benefits of DTR • Reduce the frequency of reused syringes • Reduce the syringes sharing with other
Objectives of the paper • Proportion of injections that are potentially infectious and transmit HIV (i.e. proportion infectious injection) • Which effect would be greater? • Regular • DTR+ Regular
Assumptions • Total number of syringes and the frequency of injection remain constant. • Consider only intentional injections. • Here the syringe is treated as infinitely lived.
Model I – One type of Syringe • To find out the impact of DTR in spread of HIV • How often an injection drug users (IDU’s) injects with an infectious syringe. • Kaplan [1989] introduced one type syringe model considering syringe’s perspective.
How this model differ from Kaplan’s [1989] model? • Kaplan[1989]: changes in the proportion of number of IDU's who are infected and changes in proportion of number of syringes which are infected. This paper: on the proportion of injections that are made with infectious syringes. • Kaplan[1989]: one type of syringe This paper: one and multiple types of syringes • Kaplan [1989]: followed individual syringes This paper: Sequence of syringes in succession • Kaplan [1989]: Used differential equations This paper: Discrete-time Markov model
Model I (Cont.) • Discrete-time Markov model: Find the probability that the syringe is infectious • The epochs are the instants of time just before a session in which a syringe is used to inject drugs. • At each epoch a syringe can be in two states : • Uninfectious (U) • Infectious (I) • Probability from uninfectious to infectious PUI • Probability from infectious to uninfectious PIU
Model I (Cont.) How a Un-infectious Infectious? • Used by infected user = the probability of use by an infected user • Become infectious through that use = the probability become infectious through that use • Remain infectious until just before subsequent use = probability of remain infectious until just before subsequent use. = probability that a syringe which is infectious immediately after use, ceases to be infectious before its next use.
Model I (Cont.) Probability of uninfectious syringe become infectious PUI = f φ (1- ω)
Model I (Cont.) How a infectious un infectious • Both used by an uninfected user = probability of both used by an uninfected user. Have that use render the syringe un-infectious = probability that the use renders the syringe un-infectious 2. Cease to be infectious between uses (by killing virus or replacing syringe) = probability of cease to be infectious between uses
Model I (Cont.) Probability of infectious syringe become uninfectious pUI =(1- f)θ+(1-(1-f)θ)ω) here ω = Where = probability of “dry out”/killing virus n = mean of geometric random variable
Model II • There is more than one type of syringe • The overall fraction of potentially infectious is the weighted sum of the fractions for each type of syringe. • Focus on two types of syringes. • How the proportion of infectious injections would change if DTR syringes are introduced into the current environment
Model II (Cont.) The outcome depends on: Number of both DTR and regular syringes consumed after the DTR syringes are introduced compares to the number of regular syringes consumed before DTR syringes are introduced.
Model II (Cont.) s = rate of consumption of syringes introduced by intervention/rate of consumption of regular syringes before the intervention r = change in rate of consumption of regular syringes caused by intervention/rate of consumption of regular syringes before intervention
Model II (Cont.) If the number of injections remains the same after the introduction of DTR syringes, nR=(1+r)n’R+snD where = average number of times a DTR syringe is used = average number of times a regular syringe was used before DTR syringes were introduced =average number of times regular syringes are used after DTR are introduced
Future work • Finding proportion of infectious injections for both models • Explaining properties of the model • Estimating parameter values • Numerical estimates